CRIS Current Research Information System

CERONI, FABIOLA
 Distribuzione geografica
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Continente #
NA - Nord America 557
EU - Europa 452
AS - Asia 103
AF - Africa 20
SA - Sud America 4
OC - Oceania 1
Totale 1.137
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Nazione #
US - Stati Uniti d'America 557
IT - Italia 196
GB - Regno Unito 70
SE - Svezia 59
DE - Germania 38
VN - Vietnam 28
IN - India 27
IE - Irlanda 25
CN - Cina 23
BG - Bulgaria 18
JO - Giordania 16
TG - Togo 11
RU - Federazione Russa 9
CH - Svizzera 7
FI - Finlandia 6
UA - Ucraina 6
FR - Francia 5
CI - Costa d'Avorio 4
EE - Estonia 4
ZA - Sudafrica 4
BR - Brasile 3
BE - Belgio 2
ES - Italia 2
HK - Hong Kong 2
HR - Croazia 2
NL - Olanda 2
TR - Turchia 2
AE - Emirati Arabi Uniti 1
AU - Australia 1
CL - Cile 1
IR - Iran 1
KR - Corea 1
LB - Libano 1
MD - Moldavia 1
PH - Filippine 1
SN - Senegal 1
Totale 1.137
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Città #
Chandler 72
Southend 67
Bologna 65
Fairfield 50
Ashburn 49
Redmond 32
Dublin 25
Houston 24
Princeton 24
Woodbridge 23
Sofia 18
Florence 17
New York 17
Amman 16
Wilmington 16
Seattle 15
Ann Arbor 14
Cambridge 13
Lomé 11
Milan 8
Berlin 7
Des Moines 7
San Diego 7
Boydton 6
Helsinki 6
Turin 6
Bern 5
Modena 5
Tappahannock 5
Abidjan 4
Cesena 4
Dong Ket 4
Nanjing 4
Padova 4
Shenyang 4
Westminster 4
Bari 3
Beijing 3
Guangzhou 3
Haikou 3
Salvador 3
Aversa 2
Bremen 2
Brussels 2
Dearborn 2
Ferrara 2
Hong Kong 2
Konya 2
Lausanne 2
Medford 2
Monza 2
Nanchang 2
Norwalk 2
Parma 2
Redwood City 2
Reggio Emilia 2
Rubano 2
Saint Petersburg 2
Salamanca 2
Vedelago 2
Washington 2
West Jordan 2
Amsterdam 1
Ancona 1
Anguillara Sabazia 1
Arthurs Creek 1
Boardman 1
Castel Maggiore 1
Chicago 1
Chisinau 1
Formello 1
Hangzhou 1
Hebei 1
Imola 1
Jinan 1
Kiev 1
Kuban 1
Manila 1
Olalla 1
Paris 1
Phoenix 1
Pune 1
Rome 1
Rotterdam 1
Rovigo 1
San Felice 1
Santiago 1
Seoul 1
Totale 741
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Nome #
An increased burden of rare exonic variants in NRXN1 microdeletion carriers is likely to enhance the penetrance for autism spectrum disorder. 224
A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder. 167
Contribution of CACNA1H Variants in Autism Spectrum Disorder Susceptibility 116
A deletion involving CD38 and BST1 results in a fusion transcript in a patient with autism and asthma. 96
Homozygous microdeletion of exon 5 in ZNF277 in a girl with specific language impairment. 84
null 63
New variant and expression studies provide further insight into the genotype-phenotype correlation in YAP1-related developmental eye disorders 57
Biallelic variants in the small optic lobe calpain CAPN15 are associated with congenital eye anomalies, deafness and other neurodevelopmental deficits 53
Genome-wide analysis identifies a role for common copy number variants in specific language impairment 51
Multidisciplinary investigation links backward-speech trait and working memory through genetic mutation 46
Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia 43
New GJA8 variants and phenotypes highlight its critical role in a broad spectrum of eye anomalies 43
Contribution of compound heterozygous CACNA1H mutations in autism spectrum disorder susceptibility 42
De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies 39
Reply to Pembrey et al: 'ZNF277 microdeletions, specific language impairment and the meiotic mismatch methylation (3M) hypothesis' 24
Contribution of CACNA1H variants in Autism Spectrum Disorder Susceptibility 20
Analysis of Fibroblast Growth Factor 14 (FGF14) structural variants reveals the genetic basis of the early onset nystagmus locus NYS4 and variable ataxia 16
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people 11
Discovery of 42 genome-wide significant loci associated with dyslexia 9
Totale 1.204
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Categoria #
all - tutte 3.281
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.281
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20198 0 0 0 0 0 0 0 0 0 0 5 3
2019/2020136 19 3 0 10 14 16 15 19 27 6 3 4
2020/2021200 11 4 2 1 1 2 1 30 95 14 6 33
2021/2022310 20 4 27 9 39 11 4 20 15 21 94 46
2022/2023348 23 37 16 29 18 50 20 25 70 10 37 13
2023/2024159 14 28 10 19 18 44 4 3 12 7 0 0
Totale 1.204